Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?

Ramsbottom, D; Scott, J M; Molloy, A; Weir, D G; Kirke, P N; Mills, J L; Gallagher, P M; Whitehead, A S

Ramsbottom, D; Scott, J M; Molloy, A; Weir, D G; Kirke, P N; Mills, J L; Gallagher, P M; Whitehead, A S.

Affiliation

Ramsbottom D; Department of Genetics, Trinity College, Dublin, Ireland.

Clin Genet ; 51(1): 39-42, 1997 Jan.

Article in En | MEDLINE | ID: mdl-9084933

Subject(s)

Cystathionine beta-Synthase/genetics; Homocysteine/blood; Mutation; Neural Tube Defects/genetics; Oxidoreductases Acting on CH-NH Group Donors/genetics; DNA Transposable Elements; Female; Gene Frequency; Haplotypes; Heterozygote; Homozygote; Humans; Infant, Newborn; Ireland; Methylenetetrahydrofolate Reductase (NADPH2); Neural Tube Defects/epidemiology; Polymerase Chain Reaction; Pregnancy; Risk Factors; Sequence Analysis, DNA

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Collection: 01-internacional Database: MEDLINE Main subject: Cystathionine beta-Synthase / Oxidoreductases Acting on CH-NH Group Donors / Homocysteine / Mutation / Neural Tube Defects Type of study: Etiology_studies / Risk_factors_studies Limits: Female / Humans / Newborn / Pregnancy Country/Region as subject: Europa Language: En Journal: Clin Genet Year: 1997 Document type: Article Affiliation country: Ireland Country of publication: Denmark

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